Engineering xylose metabolism in triacylglycerol-producing Rhodococcus opacusfor lignocellulosic fuel production
© Kurosawa et al.; licensee BioMed Central Ltd. 2013
Received: 6 July 2013
Accepted: 27 August 2013
Published: 16 September 2013
There has been a great deal of interest in fuel productions from lignocellulosic biomass to minimize the conflict between food and fuel use. The bioconversion of xylose, which is the second most abundant sugar present after glucose in lignocellulosic biomass, is important for the development of cost effective bioprocesses to fuels. Rhodococcus opacus PD630, an oleaginous bacterium, accumulates large amounts of triacylglycerols (TAGs), which can be processed into advanced liquid fuels. However, R. opacus PD630 does not metabolize xylose.
We generated DNA libraries from a Streptomyces bacterium capable of utilizing xylose and introduced them into R. opacus PD630. Xsp8, one of the engineered strains, was capable of growing on up to 180 g L-1 of xylose. Xsp8 grown in batch-cultures derived from unbleached kraft hardwood pulp hydrolysate containing 70 g L-1 total sugars was able to completely and simultaneously utilize xylose and glucose present in the lignocellulosic feedstock, and yielded 11.0 g L-1 of TAGs as fatty acids, corresponding to 45.8% of the cell dry weight. The yield of total fatty acids per gram of sugars consumed was 0.178 g, which consisted primarily of palmitic acid and oleic acid. The engineered strain Xsp8 was introduced with two heterologous genes from Streptomyces: xylA, encoding xylose isomerase, and xylB, encoding xylulokinase. We further demonstrated that in addition to the introduction and the concomitant expression of heterologous xylA and xylB genes, there is another molecular target in the R. opacus genome which fully enables the functionality of xylA and xylB genes to generate the robust xylose-fermenting strain capable of efficiently producing TAGs at high xylose concentrations.
We successfully engineered a R. opacus strain that is capable of completely utilizing high concentrations of xylose or mixed xylose/glucose simultaneously, and substantiated its suitability for TAG production. This study demonstrates that the engineered strain possesses a key trait of converters for lipid-based fuels production from lignocellulosic biomass.
KeywordsRhodococcus opacus Streptomyces padanus Triacylglycerol Lipid-based biofuel Lignocellulosic fuel Lignocellulosic biomass Xylose High-cell-density fermentation xylA xylB
The rises in petroleum prices along with depleting petroleum reserves have kindled a great interest in the production of bio-based alternative fuels [1–3]. Extensive discussion towards the development of clean and sustainable energy sources , especially from lignocellulosic biomass, has occurred [5, 6]. Advanced liquid (lipid-based) fuels such as gasoline, kerosene, diesel and jet fuels are of greatest interest and are expected to play a crucial role in the future global energy infrastructure [7, 8]. Triacylglycerols (TAGs) are esters in which three molecules of fatty acids are linked to glycerol, and are exploited as precursors for the production of the lipid-based biofuels [9–11]. Recently, an F-22 Raptor successfully flew on a 50/50 blend of the renewable (hydroprocessed esters and fatty acids) jet fuel and conventional petroleum-based JP-8 . Many sources of TAGs have been successfully converted to aviation biofuel and the consensus is that generally any TAGs (with the exception of those with very short chain fatty acids) are acceptable as precursors for fuel production . Therefore, these energy-rich TAG molecules have attracted much attention for developing sustainable and high-quality fuels. Currently the main sources for TAGs are vegetable oils, animal fats or waste cooking oils [13, 14]. Biofuels produced from crop seeds have come under major scrutiny due to the food vs. fuel competition issue . In addition, although algae have been considered as an attractive biocatalyst for lipid-based fuels owing to their ability to produce substantial amounts of TAGs [16, 17], it is currently estimated that large-scale production of biofuels from algae is unsustainable using existing technologies [18, 19]. Presently, the limited supply of bioresources for obtaining TAGs is a major obstacle for the production of lipid-based biofuels, in spite of the advantageous impacts that commercialization of TAG-based biofuels could provide.
R. opacus PD630, an oleaginous hydrocarbon-degrading bacterium, is able to utilize long-chain-length alkanes, acetate, phenylacetic acid, phenyldecane, propionate and gluconate and produces remarkably high amounts of TAGs as a storage material [20–22]. Although TAG production of R. opacus PD630 on glucose as a carbon source had not been shown until recently, we have demonstrated that the strain has the rare ability to accumulate large amounts of TAGs in batch-cultivations containing high concentrations of glucose under defined conditions [23, 24]. While lignocellulosic carbohydrate fractions are composed primarily of glucose, xylose represents a non-negligible portion of the sugar fraction . R. opacus PD630 is not able to utilize xylose naturally. The effective fermentation of xylose is necessary to develop economically feasible processes for fuel productions from lignocellulosic biomass [26, 27]. Expressing xylA, encoding xylose isomerase, and xylB, encoding xylulokinase, has proven to be a successful strategy to enable growth on xylose for improvement of xylose metabolism in bacteria [28–30]. Indeed, it has recently been reported that the two well-characterized genes xylA and xylB from Streptomyces lividans TK23 were expressed in R. jostii RHA1 and R. opacus PD630 to provide them with a xylose utilization capability and the role of the two genes in the Rhodococcus transformants was investigated .
Herein, we engineered a xylose-fermenting R. opacus strain capable of high-cell-density cultivation at high xylose concentrations and substantiated its usefulness for TAG production using genuine lignocellulosic hydrolysate. The present study also provides evidence for the existence of the underlying cryptic molecular target responsible for improving xylose metabolism, in addition to the expression of heterologous xylA and xylB genes, to engineer a robust xylose-fermenting Rhodococcus strain.
Metabolic engineering of R. opacusPD630 to produce TAGs on xylose
In order to engineer a xylose utilizing strain of R. opacus PD630, we sought to transfer the genes encoding enzymes essential for xylose metabolism. Streptomyces padanus MITKK-103, an actinomycete that is closely related to Rhodococcus, efficiently utilizes xylose as a sole carbon source . S. padanus genomic DNA was partially digested with the restriction enzyme Sau3AI and the DNA fragments were ligated into the BamHI site of the pAL358 plasmid bearing a gentamicin resistance cassette and an origin of replication that allows for propagation in R. opacus. R. opacus PD630 was transformed by electroporation using the resulting plasmid libraries from S. padanus. A total of 42 transformants were isolated and grown in a defined medium containing xylose as a sole carbon source. Although the cell growth and morphology of those strains on the plates were robust and similar, curiously, the capabilities of utilizing xylose and producing TAGs when grown in the flasks were different from one another. Eight strains were capable of growing in the flasks, reaching an OD660 greater than 10, and only 4 of those, termed Xsp1, 8, 10 and 12, accumulated over 30% of the cell dry weight (CDW) as TAGs (Additional file 1: Table S1).
Growth of R. opacusXsp8 with high xylose concentrations
TAG production of R. opacusXsp8 on xylose and/or glucose
Where Y is the TAG production as fatty acids (g L-1); and X1 and X2 are the uncoded values of xylose and (NH4)2SO4 concentrations (g L-1), respectively. The values of Y based on the range of X1 and X2 were calculated for all fermentations and illustrated in a response surface plot (Figure 2b). The design predicted a maximum production of fatty acids of 12.1 g L-1 by Xsp8 in the defined medium with a C/N ratio of 14.5 containing 117 g L-1 xylose and 8.08 g L-1 (NH4)2SO4. The operational C/N ratio for maximum production of fatty acids of Xsp8 on xylose was slightly lower than that of PD630 (C/N of 17.8) , the parental strain of Xsp8, on glucose.
Fermentation of R. opacusXsp8 on unbleached kraft hardwood pulp hydrolysate
Underlying molecular targets responsible for improvement of xylose metabolism in R. opacusPD630
To know whether the utilization of some sole carbon sources for growth is compared to the wild-type PD630, we assessed the differences of those strains in catabolism of 190 different substrates with the Biolog Phenotype MicroArrays . The utilization of the individual sole carbon source was expressed as the corrected average values of color development for each substrate after 5 days of incubation (Additional file 2: Figure S1). Xsp8 significantly differed from PD630 in the catabolism of only one of the tested substrates. Xylose was not utilized by PD630, but Xsp8 did catabolize xylose. The carbon source utilization profiles of these strains were essentially unchanged, although it was observed that Xsp8 was slightly impaired in its ability to utilize D-trehalose, L-valine, L-leucine and α-ketovaleric acid, relative to the parental strain.
The capability to efficiently utilize xylose as a fermentable substrate is a key attribute of microbial biocatalysts for optimizing lignocellulose-derived biofuel productions [4, 5]. Despite recent extensive efforts to develop efficient industrial biotechnological schemes for deriving biofuels from lignocelluloses, the bioconversion of xylose remains a challenge [26, 27]. Several microorganisms have been shown to grow well on xylose, but relatively few wild-type strains can utilize xylose . R. opacus PD630 is unable to catabolize xylose, as expected, although it accumulates large amounts of TAGs on glucose concentrations of more than 200 g L-1, indicating that it holds great potential as a future source of industrial biofuels derived from renewable biomass resources . Members of the genus Rhodococcus are actinomycetes and relatives of Streptomyces. We had previously disclosed that the genes from Streptomyces are functionally expressed in Rhodococcus following horizontal gene transfer from Streptomyces to Rhodococcus through competitive co-culture . In this study, we manipulated a xylose metabolic pathway in R. opacus PD630 employing genes from S. padanus MITKK-103, which utilizes xylose favourably as a sole carbon source. Consequently, we constructed a xylose-fermenting R. opacus strain Xsp8, capable of high-cell-density fermentation and TAG production under high concentrations of xylose. Xsp8 grown in batch-cultures on 120 g L-1 xylose yielded 12.0 (±1.8) g L-1 of TAGs (Figure 2). A wild-type or an engineered Rhodococcus strain capable of metabolizing xylose at greater than 100 g L-1 has not yet been reported , to our knowledge. It is well known that most microorganisms preferentially utilize glucose in a mixture of glucose and xylose due to carbon catabolite repression or allosteric competition of the sugars in sugar transport [41, 42]. Diauxic metabolism negatively impacts the process efficiency, indicating that the development of non-diauxic microbial strains is one of the main technological bottlenecks for lignocellulosic fuel production . R. opacus Xsp8 was also able to completely utilize both sugars simultaneously in a 1:1 xylose/glucose mixture for growth and TAG production. The strain exhibited a shorter lag phase compared to that on xylose alone (Figure 3). In addition, Xsp8 was completely and simultaneously able to utilize xylose and glucose present in a lignocellulosic feedstock derived from unbleached kraft hardwood pulp hydrolysate containing 70 g L-1 total sugars. The TAG production was 11.0 g L-1 as fatty acids, corresponding to 45.8% of CDW (Figure 4). Our engineered R. opacus Xsp8-strain could potentially be the most promising biocatalyst in existence for lipid-based fuels production from lignocellulosic biomass.
We also tried to identify the genes involved in improving the xylose metabolism in R. opacus PD630. The engineered strain Xsp8 was introduced with two heterologous genes from S. padanus: xylA, encoding xylose isomerase, and xylB, encoding xylulokinase (Figure 5). Intriguingly, the 3′ region of the predicted xylB gene was absent, apparently replaced by the 5′ region of a predicted cellulose-binding protein. The introduction and expression of xylA alone were sufficient to enable R. opacus PD630 to utilize xylose. The xylB gene by itself was insufficient for improving the xylose metabolism, and played a synergistic role with xylA in efficiently metabolizing xylose. The kinetics of the cellulose binding domain on xylB needs to be investigated. These findings suggest that a partly functional pathway consisting of the second step that phosphorylates D-xylulose by xylulokinase (xylB gene) in xylose metabolism is present in the parental R. opacus strain PD630. Indeed, our analysis of the whole genome sequence of R. opacus PD630 (http://www.broadinstitute.org/)  revealed two open reading frames, the predicted product of which show homology to xylulokinases. Mostly two approaches have been addressed in metabolic engineering of xylose-fermenting strains: the expression of xylose isomerase and xylulokinase, encoding xylA and xylB, respectively, or the expression of three genes encoding xylose reductase, xylitol dehydrogenase and xylulokinase [28–30, 44]. In this study, the former strategy, involving expression of the genes xylA and xylB, contributed to the improvement of xylose metabolism for R. opacus PD630. The findings are in accordance with the results that recently addressed engineering of a xylose metabolic pathway in Rhodococcus strains . Meanwhile, we suggest that there is at least one additional molecular target in the R. opacus genome which fully enables the functionality of xylA and xylB genes to generate the xylose-fermenting strain capable of efficiently producing TAGs at high xylose concentrations (Figure 6). When the plasmid pX3 (harboring xylA and xylB derived from S. padanus) was electrotransformed into the competent cells of R. opacus PD630 (wt strain) and Xsp8C (plasmid pXsp8-cured strain of Xsp8) and the resulting strains were incubated on a defined agar medium containing xylose, colonies of Xsp8C cells on the plate were larger in size than those of PD630. Additionally, the production parameters of the isolated transformants in flask culture with xylose differed significantly depending on the competent cells used between PD630 and Xsp8C. The growth and TAG production of Xsp8C-derived transformants carrying pX3 were clearly superior to those of PD630-derived transformants carrying pX3. The most probable molecular mechanism accounting for this curious phenomena may be the activation of a xylose uptake system, the mutation and expression of genes encoding xylose transporters, already present in the wild-type strain, PD630. Several xylose transporters have been found in bacteria [45, 46], including both the ABC-type transporter and xylose-proton symporter. We have not specified them at this point in R. opacus PD630, although several hypothetical proteins are annotated as possible xylose transporters in the genome of PD630 (http://www.broadinstitute.org/). Further studies are required to elucidate a mechanism of xylose uptake. These results provide important clues to develop a more robust xylose-fermenting strain for deriving low-cost biofuels from lignocellulosic biomass.
In this study, we successfully engineered a R. opacus strain that is capable of completely utilizing high concentrations of xylose or mixed xylose/glucose simultaneously and substantiated its usability for TAG production. The creation of a robust xylose-fermenting strain required the concomitant expression of xylA encoding xylose isomerase and xylB encoding xylulokinase. An engineered xylose-fermenting R. opacus strain Xsp8 was capable of completely metabolizing xylose and glucose present in unbleached kraft hardwood pulp hydrolysate containing 70 g L-1 of total sugars producing significant amounts of TAGs.
LB broth, ISP medium No.1 (tryptone-yeast extract broth), nutrient broth, yeast extract and agar were purchased from BD Diagnostic Systems (Sparks, MD). Unbleached kraft hardwood pulp was kindly provided by Old Town Fuel & Fiber (Old Town, ME). Restriction enzymes, Phusion PCR Master Mix and molecular weight markers were purchased from New England Biolabs (Ipswich, MA). The Zero Blunt TOPO PCR Cloning Kit was purchased from Invitrogen and the Geneclean II Kit was purchased from MP Biomedicals (Solon, OH), and both were used according to the manufacturers’ guidelines. All other chemicals and commercial enzymes used were obtained from Sigma-Aldrich (St. Louis, MO) unless otherwise noted.
Strains, plasmids, media and culture conditions
A list of strains and plasmids used are given in Additional file 1: Table S2. R. opacus PD630 (DSMZ 44193) was obtained from Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH. S. padanus MITKK-103 was isolated in our laboratory . One Shot TOP 10 chemically competent Escherichia coli, which was used for gene library construction and DNA manupulation, was purchased from Invitrogen (Carlsbad, CA). Plasmids pAL358 and pAL307 which carry an origin of replication and a resistance cassette of gentamicin and spectinomycin, respectively, were used as cloning vectors [47, 48].
The culture media used in this study include ISP medium No.1, LB broth, NBYE medium consisted of 8 g nutrient broth and 5 g yeast extract per liter of deionized water, and a phosphate-buffered defined medium  which contained per liter: 16 g xylose, 1.0 g (NH4)2SO4, 1.0 g MgSO4∙7H2O, 0.015 g CaCl2∙2H2O, 1.0 ml trace element solution, 1.0 ml stock A solution and 35.2 ml 1.0 M phosphate buffer. Xylose, MgSO4∙7H2O and CaCl2∙2H2O were dissolved in deionized water and sterilized by autoclaving and then stock A, trace elements, and (NH4)2SO4 were added to the cooled medium as filter sterilized stock solutions. Any modifications of the defined medium are stated in figure and table legends. Solid media were supplemented with 2% agar. In the case of plasmid-containing cultures, antibiotics were added to solid or liquid medium at the following final concentrations where appropriate: gentamicin at 10 mg L-1, spectinomycin at 100 mg L-1 or kanamycin at 50 mg L-1.
S. padanus was grown at 30°C in ISP medium No.1, and E. coli was grown at 37°C in LB broth. R. opacus strains were grown at 30°C in either LB broth or defined medium. R. opacus seed cultures for flask and fermentor cultivations were prepared in defined medium. A loopful of cells from a single colony grown on an LB agar plate for 3 days was used to inoculate 50 ml of defined medium in a 250-ml baffled flask. The culture was then incubated on a rotary shaker (200 rpm) until it reached an optical density (OD660) of 15, as determined by a Spectronic 20 Genesys spectrophotometer (Spectronic Instruments). Shake flask experiments were carried out using 250-ml baffled flasks containing 50 ml of defined medium incubated on a rotary shaker (200 rpm) at 30°C. Unless otherwise stated, cultures were inoculated with a seed culture to an initial OD660 of about 0.3 (7.5 × 107 cfu mL-1). Fermentor experiments were performed with a Sixfors bioreactor system (Infors) as previously described . Unless otherwise stated, fermentor-cultures were inoculated with the seed culture at an initial OD660 of 1.0.
Experimental design and statistical analysis for medium optimization
The operational C/N ratio of the medium for maximum production of fatty acids was optimized using a response surface methodology based on the Box-Wilson Central Composition Design . The design matrix of the experimental conditions was subjected to regression analysis by using the software StatGraphics (StatPoint). The design class chosen to carry out the experiments was a response surface with 11 proofs and a triplicate central point.
DNA manipulations were carried out using established methods , and used following the manufacturers’ instructions. Genomic DNAs from S. padanus and R. opacus were prepared as previously described [32, 47]. PCR amplifications were performed with a Bio-Rad C1000 Thermal Cycler using Phusion High-Fidelity PCR kits. Plasmids were purified with Perfectprep plasmid mini kits. DNA fragments were recovered from agarose gels by using Geneclean II kits. Primers used in this study are described in Additional file 1: Table S3. DNA sequencing was carried out by using an Applied Biosystems Model 3730 DNA sequencer at the MIT Biopolymers Laboratory. The open reading frame (ORF) identification and similarity searches of nucleotide and protein sequences were performed using the BLASTN, BLASTX, BLASTP and ORF Finder programs from the NCBI website (http://blast.ncbi.nlm.nih.gov/Blast.cgi). Multiple sequence alignments were done with the program CLUSTALW (http://www.genome.jp/tools/clustalw/).
Construction of S. padanusgenomic DNA library and plasmids
For S. padanus plasmid library, genomic DNA of S. padanus MITKK-103 was partially digested with Sau3AI, and electrophoresed on an agarose gel (0.7%). The digested fragments ranging from 2 to 6 kbp were excised from the agarose gel, purified, ligated with BamHI-digested pAL358 vector and transformed into E. coli TOP10 competent cells. The cells were plated onto LB plates containing gentamicin, and approximately 30,000 colonies were scraped off the plates after 24 h of cultivation. The plasmid library was purified and used to transform into R. opacus.
For plasmid pX1, the DNA fragment encoding xylA gene was PCR-amplified from pXsp8 using a pair of primers 3603-xylA-U and 3603-xylA-D1, which incorporated BamHI and SpeI restriction sites. The PCR product was cloned into pCR-Blunt II-TOPO and proliferated in E. coli TOP10 competent cells. Positive clones were identified through selection on LB plates containing kanamycin and 50 mg L-1 of X-gal (5-bromo-4-chloro-indolyl-β-D-galactopyranoside). The plasmids were isolated and digested with BamHI and SpeI for ligation into pAL307 vector, which was similarly digested. The 1475-bp fragment and digested pAL307 were purified, and cohesive end ligations were carried out with T4 DNA ligase. The ligation mixtures were again transformed into E. coli TOP10 cells, and the positive clones were identified through selection on LB plates containing spectinomycin, and pX1 was isolated. For plasmid pX2, the fragment encoding xylB gene was amplified from pXsp8 using a pair of primers 3603-xylB-U1 and 3603-xylB-D, which incorporated BamHI and SpeI restriction sites. The product was digested with BamHI and SpeI and the resulting 2064-bp fragment was cloned into BamHI-SpeI-digested pAL307, as described above, creating pX2. For plasmid pX3, the fragment encoding xylA gene was amplified from pXsp8 using a pair of primers 3603-xylA-U and 3603-xylA-D2, which incorporated BamHI and PstI restriction sites. The product was digested with BamHI and PstI (fragment 1). The DNA encoding xylB gene was amplified from pX2 using a pair of primers 3603-xylB-U2 and 3603-xylB-D, which incorporated PstI and SpeI restriction sites. The product was digested with PstI and SpeI (fragment 2). Fragments 1 and 2 were then ligated together with T4 DNA ligase, and the ligated fragment was purified from an electrophoresed agarose gel. The 3902-bp fragment was cloned into BamHI-SpeI-digested pAL307, creating pX3. For plasmid pX4, the fragment encoding xylA gene was amplified from pXsp8 using a pair of primers 3603-xylA-U and 3603-xylA-D2, which incorporated BamHI and PstI restriction sites. The product was digested with BamHI and PstI (fragment 3). The DNA encoding xylB gene without cellulose-binding domain was amplified from pX2 using the primers 3603-xylB-U2 and 3603-xylB#-D, which incorporated PstI and SpeI restriction sites. The product was digested with PstI and SpeI (fragment 4). Fragments 3 and 4 were ligated, and the resulting 3191-bp fragment was cloned into BamHI-SpeI-digested pAL307, creating pX4. For plasmid pX0, the fragment of an untranslated region noncoding xylA and/or xylB genes was amplified from pXsp8 using a pair of primers 3603-xylA-U and 3603-dele-D, which incorporated BamHI and SpeI restriction sites. The product was digested with BamHI and SpeI, and the resulting 125-bp fragment was cloned into BamHI-SpeI-digested pAL307, creating pX0.
Electroporation of R. opacus
R. opacus electrocompetent cells of PD630 and Xsp8C (plasmid-cured strain of Xsp8) were prepared as previously described . Xsp8C was obtained by consecutively passaging individual colonies of Xsp8 on LB plates and testing for sensitivity to gentamicin and plasmid loss using agarose gel electrophoresis. S. padanus plasmid library, pX0, pX1, pX2, pX3 or pX4 were introduced into PD630 or Xsp8C by electroporation using a Bio-Rad Gene Pulser. Immediately before the electroporation, 70 μl of competent cells were mixed with the plasmid DNA (50~500 ng). The electrotransformation was performed in a 2 mm electroporation cuvette (VWR North American) and electroporated at 2.5 kV, 25 μF and 200 Ω. Pulsed cells were diluted with 300 μl of LB broth, regenerated for 3 h with gentle agitation, plated onto defined xylose plates containing gentamicin or spectinomycin and incubated to identify xylose utilizing transformants.
Cell growth was followed by measurement of the optical density at 660 nm (Thermo Scientific GENESYS 20) or cell dry weight (CDW). The CDW was determined after lyophilization of cells obtained by centrifuging 10 ml of culture broth at 8,000 g for 15 min. The lyophilized cell pellet was analyzed for the fatty acid concentrations. The supernatants of the culture broth were analysed for residual sugars and (NH4)2SO4. The residual sugar concentrations were measured by high-performance liquid chromatography (HPLC) as previously described . Residual ammonia concentrations were determined by the Ammonia Assay kit (Sigma-Aldrich) according to the manufacturer’s instructions. For the analysis of total lipids, fatty acids were converted to methyl esters (FAMEs) by methanolysis followed by gas chromatography (GC) as previously described . The fatty acids were identified and quantified by comparison to standard FAMEs. Fatty acid content was defined as the percentage of the ratio of fatty acids to cell dry weight (% CDW).
Saccharification of unbleached kraft hardwood pulp
Enzymatic saccharification was performed in 2 liter flasks at 45°C on a rotary shaker at 200 rpm. Lignocellulose-degrading enzymes loaded were Pentopan, Viscozyme (23 mg protein mL-1, determined by Bio-Rad protein assay), Celluclast (48 mg protein mL-1) and Novozyme 188 (57 mg protein mL-1). At given duration times, the slurry was withdrawn, centrifuged at 8,000 g for 20 min and the supernatant was used for subsequent analysis and fermentation.
Phenotypic testing of carbon source utilization
Carbon assimilation profiles of the strains were evaluated using Phenotype MicroArray PM1 & 2 carbon panels (Biolog) by following the manufacturer’s instructions . The reduction of the redox dye tetrazolium during respiration due to carbon catabolism causes the formation of a purple color in the well. Following incubation, the utilization of the sole substrates was measured spectrophotometrically at 595 nm, using a FLUOstar OPTIMA plate reader (BMG Labtech).
The nucleotide sequences of pXsp8, pX0, pX1, pX2, pX3 and pX4 reported in this study were deposited in the GenBank database under accession numbers KC817027, KC817028, KC817029, KC817030, KC817031 and KC817032, respectively.
Cell dry weight
Carbon to nitrogen ratio
Open reading frame
Polymerase chain reaction
High performance liquid chromatography
Fatty acid methyl ester.
This work was supported by Shell Global Solutions Inc., Logos Technologies, Inc., and a seed grant from the MIT Energy Initiative. The authors would like to thank C. Anthony Debono and Jil C. Ulrich for technical assistances, and Christopher J. Brigham for a critical review of the manuscript.
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